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fr3.trackDb.html : Differences exist between hgwbeta and hgw2 

(RR fields taken from public MySql server, not individual machine)

7968,7980d7967
< rmsk | <p>
< rmsk | When analyzing the data tables of this track, keep in mind that Repbase is not the same 
< rmsk | as the Repeatmasker sequence database and that the repeat names in the
< rmsk | Repeatmasker output are not the same as the sequence names in the Repeatmasker
< rmsk | database.  Concretely, you can find a name such as "L1PA4" in the Repeatmasker
< rmsk | output and this track, but there is not necessarily a single sequence "L1PA4"
< rmsk | in the Repeatmasker database. This is because Repeatmasker creates annotations
< rmsk | by joining matches to partial pieces of the database together so there is no
< rmsk | 1:1 relationship between its sequence database and the annotations. To learn
< rmsk | more, you can read the Repeatmasker paper, its source code or reach out to the
< rmsk | Repeatmasker authors, your local expert on transposable elements or us.
< rmsk | </p>
< rmsk | 

9069,9074c9056,9059
< uniprot | Features in the &quot;UniProt Modifications&quot; (modified residues) track are drawn in 
< uniprot |  <span style="color: rgb(200,200,0)"><b>light green</b></span>. Disulfide bonds are shown in 
< uniprot |  <span style="color: rgb(100,100,100)"><b>dark grey</b></span>. Topological domains
< uniprot |  in <span style="color: rgb(100,0,0)"><b>maroon</b></span> and zinc finger regions in 
< uniprot |  <span style="color: rgb(100,100,0)"><b>olive green</b></span>.
< uniprot | </p>
---
> uniprot | In the &quot;UniProt Modifications&quot; track, lipoification sites are highlighted in 
> uniprot | <span style="color: rgb(12,12,120)"><b>dark blue</b></span>, glycosylation sites in 
> uniprot | <span style="color: rgb(0,100,100)"><b>dark green</b></span>, and phosphorylation in 
> uniprot | <span style="color: rgb(200,200,0)"><b>light green</b></span>.</p>